Efficacy of Oral Ciprofloxacin in acute endophthalmitis prophylaxis

Phase 2

• Conditions: Condition 1: Purulent Endophthalmitis. Condition 2: Open globe injury.; Panophthalmitis Vitreous abscess; Penetrating wound of orbit with or without foreign body

• Registration Number: IRCT2014060818004N1
• Lead Sponsor: Vice chancellor for research , Zahedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Inclusion criteria : The need for acute endophthalmitis prophylaxis ; living in Zahedan
Exclusion criteria : All patients who have had eye surgery and other eye diseases ; single-eye patients ; patients who are undergoing medical treatment ; less than 18 years of age ; suspicion for fungal infection ; severe infection

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Acute endophthalmitis onset. Timepoint: one week. Method of measurement: examination.

Secondary Outcome Measures

Name	Time	Method
Oral ciprofloxacin adverse effects. Timepoint: 1 week. Method of measurement: history and examination.;IV cefazolin and gentamicin adverse effects. Timepoint: 1 week. Method of measurement: history , examination and lab test.